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31.
In the present work, an innovative leach proof nanocatalyst based on dendritic fibrous nanosilica (DFNS) modified with ionic liquid loaded Fe3O4 NPs and CuI salts was designed and applied for the rapid synthesis of imidazo[1,2‐a]pyridines from the reaction of phenyl acetylene, 2‐aminopyridine, and aldehydes in aqueous medium. The structure of the synthesized nanocatalyst was studied by field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), Fourier transform infrared (FT‐IR), flame atomic absorption spectroscopy (FAAS), energy‐dispersive X‐ray (EDX), and X‐ray diffraction (XRD), vapor–liquid–solid (VLS), and adsorption/desorption analysis (Brunauer–Emmett–Teller [BET] equation) instrumental techniques. CuI/Fe3O4NPs@IL‐KCC‐1 with high surface area (225 m2 g?1) and porous structure not only exhibited excellent catalytic activity in aqueous media but also, with its good stability, simply recovered by an external magnet and recycled for eight cycles without significant loss in its intrinsic activity. Higher catalytic activity of CuI/Fe3O4NPs@IL‐KCC‐1 is due to exceptional dendritic fibrous structure of KCC‐1 and the ionic liquid groups that perform as strong anchors to the loaded magnetic nanoparticles (MNPs) and avoid leaching them from the pore of the nanocatalyst. Green reaction media, shorter reaction times, higher yields (71–97%), easy workup, and no need to use the chromatographic column are the advantages of the reported synthetic method.  相似文献   
32.
The authors describe a 3-component nanoparticle system composed of a silica-coated magnetite (Fe3O4) core and a layered double (Cu-Cr) hydroxide nanoplatelet shell. The sorbent has a high anion exchange capacity for extraction anionic species. A simple online system, referred to as "on-line packed magnetic-in-tube solid phase microextraction" was designed. The nanoparticles were placed in a stainless steel cartridge via dry packing. The cartridge was then applied to the preconcentration acidic drugs including naproxen and indomethacin from urine and plasma. Extraction and desorption times, pH values of the sample solution and flow rates of sample solution and eluent were optimized. Analytes were then quantified by HPLC with UV detection. Under optimal conditions, the limits of detection range from 70 to 800 ng L?1, with linear responses from 0.1–500 μg L?1 (water samples), 0.6–500 μg L?1 (spiked urine), and 0.9–500 μg L?1 (spiked plasma). The inter- and intra-assay precisions (RSDs, for n?=?5) are in the range of 2.2–5.4%, 2.8–4.9%, and 2.0–5.2% at concentration levels of 5, 25 and 50 μg L?1, respectively. The method was applied to the analysis of the drugs in spiked human urine and plasma, and good results were achieved.
Graphical abstract Fe3O4@SiO2@CuCr-LDH magnetic nanoparticles were synthesized and packed in to a stainless steel column. The column was applied to solid phase microextraction of acidic drugs from biological samples.
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33.
In the present study, a simple versatile extraction method based on supramolecular solvent microextraction followed by inductively coupled plasma atomic emission spectrometry was developed for the extraction, separation and determination of zirconium (Zr) from hafnium (Hf). Zr and Hf were complexed with bis(2,4,4-trimethylpentyl) phosphinic acid, to obtain hydrophobic complex, and extracted into supramolecular solvent phase. The effective parameters on the supramolecular solvent microextraction efficiency were studied and optimized by using two different optimization methods: one variable at a time and central composite design. Under the optimum conditions, the linear range of 0.3–200.0 and 2.0–200.0 µg L?1, detection limits (S/N = 3) of 0.1 and 0.6 µg L?1, and precisions (n = 5) of 3.2–4.9% and 3.0–5.1% were obtained for Zr and Hf, respectively. Finally, the proposed method has been successfully applied for the extraction and separation of these cations in zirconium ore sample.  相似文献   
34.
Novel quinolone derivatives featuring an 1,3,4-oxadiazole ring as a metal-chelating component and a benzyl group base on HIV-1 integrase inhibitors pharmacophore were designed and synthesized. An antiviral assay revealed that most analogues inhibited HIV-1 replication in the cell culture. Our results showed that compounds bearing small alkyl groups as R group were inactive in anti-HIV-1 assay, whereas compounds possessing benzyl or substituted benzyl at the same position showed good anti-HIV activity with the range of 20–57% at 100 μM concentration. Among them, 3-(5-((2-fluorobenzyl)thio)-1,3,4-oxadiazol-2-yl)-8-phenylquinolin-4-(1H)-one (compound 13) showed reasonable cell-based antiviral activity (EC50 = 50 μM) with no considerable cytotoxicity (CC50 > 100 μM) in the cell viability assay, suggesting that it may be amenable to further development for identifying new anti-HIV-1 agents. Docking studies using the later crystallographic data available for PFV integrase corroborate favorable binding to the active site of HIV integrase, providing a basis for the design of more potent analogues.  相似文献   
35.

In this study, the corrosion behavior of Zircaloy was investigated in the presence and absence of copper–graphene nanocomposites coating. The coating was prepared employing Hummers’ and electrochemical reduction methods. The morphology of copper–graphene nanocomposites coating was studied using scanning electron microscopy (SEM). Corrosion behavior was investigated employing dynamic polarization and electrochemical impedance spectroscopy (EIS) tests in a solution containing lithium hydroxide (LiOH), boric acid (H3BO3), and deionized water. The results showed that corrosion resistance of Zircaloy increased with introduction of copper–graphene nanocomposites coatings. The lowest corrosion rate was attained in the Zircaloy with copper–graphene nanocomposites coating (corrosion rate: 0.040 mm/year). An approximately 20 times decrease in the corrosion rate was observed in the Zircaloy with copper–graphene nanocomposites coating when compared to the un-coated Zircaloy (corrosion rate: 0.831 mm/year).

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36.
A new method to realize a discrete memristor is proposed. The device under study consists of a tube filled of aqueous saturated solution of copper sulfate which can be electrolyzed by using two asymmetric copper electrodes, one of which has a considerably smaller cross-sectional area than to the other one. It is shown both theoretically and experimentally that this device has exactly the properties of a memristor if it is designed such that the electrical field and the current density on the thinner electrode when it acts as anode are sufficiently large. Different aspects of the proposed discrete memristor, including pinched hysteresis loop, on-off resistance ratio and memory volatilization, are studied and experimental results are presented.  相似文献   
37.
Synthesis of novel hybrid derivatives of two known scaffolds, pyrrolidine-2-one and piperazine, is described. Initially, the Ugi reaction of phenylglyoxal, aromatic amines, coumarin-3-carboxylic acid and isocyanides in methanol resulted in the formation of dihydrochromeno[3,4-c]pyrrole-3,4-diones. The obtained products were then treated with N-alkylpiperazines in dichloromethane to afford the novel N-substituted pyrrolidine-2-one containing piperazine derivatives in satisfactory yields. The proof of the structures was carried out by means of spectroscopic information and X-ray crystallography.  相似文献   
38.
We present some iterative methods of different convergence orders for solving systems of nonlinear equations. Their computational complexities are studies. Then, we introduce the method of finite difference for solving stochastic differential equations of Itô-type. Subsequently, our multi-step iterative schemes are employed in this procedure. Several experiments are finally taken into account to show that the presented approach and methods work well.  相似文献   
39.
40.
Single phase nanocrystalline La0.6Ca0.4MnO3 powder was synthesized by both the usual and a modified citrate gel precursor method, and the effects on the formation of homogeneous nano-sized powder with a perovskite structure were investigated. In the modified method, single phase La0.6Ca0.4MnO3 powder with an average particle size of 17.2 nm was obtained when the powder was pyrolyzed at 520°C for 2 h. Its specific surface area was 40.7 m2 g−1, about 4-fold larger than that of powder made by the usual citrate gel method.   相似文献   
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